EFFECTS OF CARBON SOURCES ON SECONDARY METABOLITES BIOSYNTHESIS BY Fusarium verticillioides

ACHIMÓN F; JACQUAT, AG; BRITO VD; DAMBOLENA J.S.; ZYGADLO JA; PIZZOLITTO RP

Buenos Aires

Congreso; XX ANNUAL MEETING OF THE ARGENTINEAN BIOLOGY SOCIETY (SAB); 2018

SOCIEDAD ARGENTINA DE BIOLOGIA

Fusarium verticillioides is one of the most important fungal pathogens of maize, being responsible of major economic losses worldwide due to its effect on grain quality and mycotoxincontamination, particularly fumonisin B1 (FB1 ), which is extremely harmful to human and animal health. Secondary metabolites (SMs) production often occurs during stationary phase. F. verticillioides SMs include toxins such as FB1, volatile organic compounds such as sesquiterpenes (SQT) and pigments (naphthoquinones), among other metabolites. The aim of the present study was to determine the effect of different carbon sources, consisting of glucose, sucrose, lactose, fructose or xylose, on vegetative growth and secondary metabolism in F. verticillioides. For evaluation of growth, F.verticillioides M3125 was incubated at 28°C in Czapek Dox Agar (CDA) supplemented with different carbon sources. For evaluation of secondary metabolites, liquid GYAM medium was used (adjusted to pH 3) and cultures were incubated with shaking at 25°C for 7 days. At the end of the incubation period, pH value was registered, FB1 quantification was performed using a HPLC, SQTquantification was carried out using a GC-MS and total naphthoquinones were quantified with a spectrophotometer. Lower lag phase values were achieved with lactose and sucrose as carbon sources (both disaccharides), compared to glucose, xylose and fructose (monosaccharides). This may be explained by the development of more extended andpoor branched hyphae when the fungus grows with disaccharides as carbon sources. This may be a strategyto explore the surrounding media for areas with simpler carbohydrates. The growth rate was higher with fructose and conidiation was higher with lactose. FB1 biosynthesis was statistically higher with sucrose and glucose (both with pH 3.5) and lower with xyloseand fructose. On the other hand, naphthoquinone biosynthesis wasstatistically higher with fructose (pH 3.7) followed by xylose (pH 4.8), while lower values were achieved with glucose and sucrose. Lactose did not support the biosynthesis of these SMs. On the other hand, SQT biosynthesis was statistically higher with xylose compared to the other carbon sources. According to our results, growing parameters, conidiation and biosynthesis of secondarymetabolites are regulated by both environmental (pH) and nutritional factors (carbon source). Also, our results suggest an inverse relationship between FB1 and naphthoquinones biosynthesis. It is well documented that both metabolites proceed via the polyketide route by formation of a common precursor. In addition, there are global and specific regulators that respond to environmental signals and activate one of the metabolites while repressing the other.SQT production does not show a pattern with the other SMs studied. In fact, its biosynthesis proceeds through a different pathway, the mevalonic acid pathway. It has been proposed that trichodiene synthase activity (the enzyme involved in the first step of SQT biosynthesis) is optimum at pH values near 6, which could explained the higher amount of SQT produced with xylose as carbon source (pH 4.8). However, xylose itself could represent a signal that induces SQTbiosynthesis.